Closed-Loop Insulin Delivery Versus Sensor-Augmented Pump Therapy in Older Adults With Type 1 Diabetes (ORACL): A Randomized, Crossover Trial.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
01 02 2022
Historique:
received: 09 08 2021
accepted: 01 11 2021
pubmed: 1 12 2021
medline: 11 3 2022
entrez: 30 11 2021
Statut: ppublish

Résumé

To assess the efficacy and safety of closed-loop insulin delivery compared with sensor-augmented pump therapy among older adults with type 1 diabetes. This open-label, randomized (1:1), crossover trial compared 4 months of closed-loop versus sensor-augmented pump therapy. Eligible adults were aged ≥60 years, with type 1 diabetes (duration ≥10 years), using an insulin pump. The primary outcome was continuous glucose monitoring (CGM) time in range (TIR; 3.9-10.0 mmol/L). There were 30 participants (mean age 67 [SD 5] years), with median type 1 diabetes duration of 38 years (interquartile range [IQR] 20-47), randomized (n = 15 to each sequence); all completed the trial. The mean TIR was 75.2% (SD 6.3) during the closed-loop stage and 69.0% (9.1) during the sensor-augmented pump stage (difference of 6.2 percentage points [95% CI 4.4 to 8.0]; P < 0.0001). All prespecified CGM metrics favored closed loop over the sensor-augmented pump; benefits were greatest overnight. Closed loop reduced CGM time <3.9 mmol/L during 24 h/day by 0.5 percentage points (95% CI 0.3 to 1.1; P = 0.0005) and overnight by 0.8 percentage points (0.4 to 1.1; P < 0.0001) compared with sensor-augmented pump. There was no significant difference in HbA1c between closed-loop versus sensor-augmented pump stages (7.3% [IQR, 7.1-7.5] (56 mmol/mol [54-59]) vs. 7.5% [7.1-7.9] (59 mmol/mol [54-62]), respectively; P = 0.13). Three severe hypoglycemia events occurred during the closed-loop stage and two occurred during the sensor-augmented pump stage; no hypoglycemic events required hospitalization. One episode of diabetic ketoacidosis occurred during the sensor-augmented pump stage; no serious adverse events occurred during the closed-loop stage. Closed-loop therapy is an effective treatment option for older adults with long-duration type 1 diabetes, and no safety issues were identified. These older adults had higher TIR accompanied by less time below range during closed loop than during sensor-augmented pump therapy. Of particular clinical importance, closed loop reduced the time spent in hypoglycemic range overnight.

Identifiants

pubmed: 34844995
pii: dc21-1667
doi: 10.2337/dc21-1667
doi:

Substances chimiques

Blood Glucose 0
Hypoglycemic Agents 0
Insulin 0

Banques de données

ANZCTR
['ACTRN12619000515190']
figshare
['10.2337/figshare.16924480']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

381-390

Informations de copyright

© 2022 by the American Diabetes Association.

Auteurs

Sybil A McAuley (SA)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

Steven Trawley (S)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Psychology, Cairnmillar Institute, Melbourne, Australia.

Sara Vogrin (S)

Department of Medicine, The University of Melbourne, Melbourne, Australia.

Glenn M Ward (GM)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

Spiros Fourlanos (S)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Diabetes and Endocrinology, The Royal Melbourne Hospital, Melbourne, Australia.

Charlotte A Grills (CA)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

Melissa H Lee (MH)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

Andisheh Mohammad Alipoor (AM)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

David N O'Neal (DN)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

Niamh A O'Regan (NA)

Department of Geriatric Medicine, Waterford Integrated Care for Older People, University Hospital Waterford, Waterford, Ireland.

Vijaya Sundararajan (V)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Public Health, La Trobe University, Melbourne, Australia.

Peter G Colman (PG)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Diabetes and Endocrinology, The Royal Melbourne Hospital, Melbourne, Australia.

Richard J MacIsaac (RJ)

Department of Medicine, The University of Melbourne, Melbourne, Australia.
Department of Endocrinology & Diabetes, St Vincent's Hospital Melbourne, Melbourne, Australia.

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Classifications MeSH